FDA applicant

Professional Positioners, Inc.

Racine, WI3 decisions1993–19950 recalls

FDA records 3 decisions for Professional Positioners, Inc. (Racine, WI) from 1993 to 1995: 3 510(k) clearances. Most are in product codes EBI (Resin, Denture, Relining, Repairing, Rebasing) and DZB (Headgear, Extraoral, Orthodontic). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Professional Positioners, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Professional Positioners, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Professional Positioners, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Professional”

FDA records each applicant name separately; these may or may not be the same firm.

Professional Medical Services 19 Professional Medical Products, Inc. 9 Professional Latex Sdn Bhd 3 Professional Instruments Co. 3 Professional Tape Co., Inc. 2 Professional Services For Surgeons, Ltd. 2 Professional Dental Mfg., Inc. 2 Professional Technologies Corp. 2 Professional Supplies, Inc. 2 Professional Disposables International, Inc. 1 Professional Medical Systems 1 Professional Pharmacy West, Inc. 1

Professional Positioners, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Professional”